Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/T
Location

Chromosome 8: between 23026275 and 23026276 (forward strand) | View in location tab

Most severe consequence

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 8 individual genotypes.

Variation displays